Product Details

SNP ID

rs114133800

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:39008438 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CGGCTCTGTTTTTGCCTTTTTGTTA[A/C]AAAATCAGTATGTCTCATTCGGTCA

Phenotype

MIM: 609099

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

FBXO27 PubMed Links

Additional Information

For this assay, SNP(s) [rs201539158] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

FBXO27

Gene Name

F-box protein 27

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_178820.4		Intron			NP_849142.1
XM_017026290.1		Intron			XP_016881779.1

View Full Product Details